BEUDAMED
    10 results · 22ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Adverse Event ×

    IOLMASTER 700

    FDA Adverse Event
    Malfunction ·CARL ZEISS MEDITEC AG (JENA)·Product code HJO·January 19, 2024

    IOLMASTER 700

    FDA Adverse Event
    Injury ·CARL ZEISS MEDITEC AG (JENA)·Product code HJO·September 22, 2017

    IOLMASTER 700

    FDA Adverse Event
    Injury ·CARL ZEISS MEDITEC AG (JENA)·Product code HJO·September 22, 2017

    TRANSTAR STRETCHER

    FDA Adverse Event
    Malfunction ·HILLROM DE MEXICO S DE RL DE CV·Product code FPO·April 3, 2014

    ACCU-CHEK SPIRIT COMBO

    FDA Adverse Event
    Malfunction ·ROCHE HEALTH SOLUTIONS, INC.·Product code LZG·January 18, 2013

    COLLAMER ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER SINGLE PIECE FOLDABLE INTRAOCUL

    FDA Adverse Event
    Malfunction ·STAAR SURGICAL CO.·Product code HQL·December 8, 2010

    IOLMASTER 700

    FDA Adverse Event
    Injury ·CARL ZEISS MEDITEC AG (JENA)·Product code HJO·May 5, 2017

    IOLMASTER 700

    FDA Adverse Event
    Injury ·CARL ZEISS MEDITEC AG (JENA)·Product code HJO·July 12, 2017

    IOLMASTER 700

    FDA Adverse Event
    Injury ·CARL ZEISS MEDITEC AG (JENA)·Product code HJO·July 3, 2016

    IOLMASTER 700

    FDA Adverse Event
    Injury ·CARL ZEISS MEDITEC AG (JENA)·Product code HJO·July 3, 2016